Canonical Allele Identifier: CA460497004
Gene: STAR HGNC NCBI

Linked Data

MyVariant Identifiers: chr8:g.38003639T>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.38146121T>A , CM000670.2:g.38146121T>A GRCh38
NC_000008.10:g.38003639T>A , CM000670.1:g.38003639T>A GRCh37
NC_000008.9:g.38122796T>A NCBI36
NG_011827.1:g.9962A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000276449.9:c.492A>T MANE Select ENSP00000276449.3:p.Thr164=
ENST00000276449.8:c.492A>T ENSP00000276449.3:p.Thr164=
ENST00000520114.1:n.979A>T
ENST00000522050.1:c.428A>T
NM_000349.2:c.492A>T NP_000340.2:p.Thr164=
XM_006716392.1:c.492A>T XP_006716455.1:p.Thr164=
NM_000349.3:c.492A>T MANE Select NP_000340.2:p.Thr164=
Search 100 bp 5'
Search 100 bp 3'